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Analysis of the antimicrobial mechanism of porcine beta defensin 2 against E. coli by electron microscopy and differentially expressed genes

机译:猪β防御素2对大肠杆菌的抗菌作用的电子显微镜和差异表达基因分析

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摘要

Porcine beta defensin 2 (pBD2) is a cationic antimicrobial peptide with broad spectrum antibacterial activity, which makes it a potential alternative to antibiotics to prevent and cure diseases of pigs. However, development of pBD2 as an effective antibiotic agent requires molecular understanding of its functional mechanism against pathogens. In this study, we investigated the functional mechanism of pBD2 antibacterial activity. Escherichia coli was incubated with different pBD2 concentrations for different times. Electron microscopy was used to analyze the locations of pBD2 and its induced morphological changes in E. coli. Gene expression analysis was also performed to further understand the molecular changes of E. coli in response to pBD2 incubation. The results demonstrated that E. coli membranes were broken, holed, and wrinkled after treatment with pBD2, and pBD2 was located on the cell membranes and manly in the cytoplasm. Furthermore, 38 differentially expressed genes (DEGs) were detected, successfully sequenced and confirmed by quantitative real-time PCR (qRT-PCR). Most of the known functional DEGs were associated with DNA transcription and translation and located in the cytoplasm. Collectively, the results suggest that pBD2 could have multiple modes of action and the main mechanism for killing E. coli might be influence on DNA transcription and translation by targeting intracellular molecules after membrane damage, although transport and metabolism proteins were also affected.
机译:猪β防御素2(pBD2)是一种具有广谱抗菌活性的阳离子抗菌肽,使其成为预防和治疗猪疾病的抗生素的潜在替代品。然而,将pBD2开发为有效的抗生素需要分子了解其抗病原体的功能机制。在这项研究中,我们调查了pBD2抗菌活性的功能机制。将大肠杆菌与不同浓度的pBD2孵育不同的时间。电子显微镜用于分析pBD2的位置及其在大肠杆菌中的诱导形态变化。还进行了基因表达分析以进一步了解响应pBD2孵育的大肠杆菌分子变化。结果表明,用pBD2处理后,大肠杆菌膜破裂,破洞,起皱,pBD2位于细胞膜上,男子气概位于细胞质中。此外,通过定量实时PCR(qRT-PCR)检测到38个差异表达基因(DEG),成功对其进行了测序和确认。大多数已知的功能性DEG与DNA转录和翻译有关,并位于细胞质中。总的来说,这些结果表明pBD2可能具有多种作用方式,并且杀死大肠埃希菌的主要机制可能是通过靶向破坏膜后的细胞内分子来影响DNA转录和翻译,尽管转运和代谢蛋白也受到了影响。

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